WO2022243867A2 - Raccordement fluidique de trajets d'échantillonnage et de séparation - Google Patents

Raccordement fluidique de trajets d'échantillonnage et de séparation Download PDF

Info

Publication number
WO2022243867A2
WO2022243867A2 PCT/IB2022/054575 IB2022054575W WO2022243867A2 WO 2022243867 A2 WO2022243867 A2 WO 2022243867A2 IB 2022054575 W IB2022054575 W IB 2022054575W WO 2022243867 A2 WO2022243867 A2 WO 2022243867A2
Authority
WO
WIPO (PCT)
Prior art keywords
sampling
mobile phase
drive
sample
separating device
Prior art date
Application number
PCT/IB2022/054575
Other languages
English (en)
Other versions
WO2022243867A3 (fr
Inventor
Thomas Ortmann
Dominik Ruf
Original Assignee
Agilent Technologies, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agilent Technologies, Inc. filed Critical Agilent Technologies, Inc.
Publication of WO2022243867A2 publication Critical patent/WO2022243867A2/fr
Publication of WO2022243867A3 publication Critical patent/WO2022243867A3/fr

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/04—Preparation or injection of sample to be analysed
    • G01N30/16—Injection
    • G01N30/20—Injection using a sampling valve
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/04—Preparation or injection of sample to be analysed
    • G01N30/16—Injection
    • G01N30/20—Injection using a sampling valve
    • G01N2030/201—Injection using a sampling valve multiport valves, i.e. having more than two ports
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
    • G01N30/04—Preparation or injection of sample to be analysed
    • G01N30/16—Injection
    • G01N30/20—Injection using a sampling valve
    • G01N2030/202—Injection using a sampling valve rotary valves

Definitions

  • the present invention relates to fluidic coupling of sampling and separation path, in particular for chromatographic sample separation.
  • HPLC high performance liquid chromatography
  • a liquid has to be provided usually at a very controlled flow rate (e. g. in the range of microliters to milliliters per minute) and at high pressure (typically 20-100 MPa, 200-1000 bar, and beyond up to currently 200 MPa, 2000 bar) at which compressibility of the liquid becomes noticeable.
  • a mobile phase comprising a sample fluid (e.g. a chemical or biological mixture) with compounds to be separated is driven through a stationary phase (such as a chromatographic column packing), thus separating different compounds of the sample fluid which may then be identified.
  • a sample fluid e.g. a chemical or biological mixture
  • stationary phase such as a chromatographic column packing
  • the mobile phase for example a solvent
  • a chromatographic column containing packing medium also referred to as packing material or stationary phase.
  • packing medium also referred to as packing material or stationary phase.
  • the different compounds each one having a different affinity to the packing medium, move through the column at different speeds.
  • Those compounds having greater affinity for the stationary phase move more slowly through the column than those having less affinity, and this speed differential results in the compounds being separated from one another as they pass through the column.
  • the stationary phase is subject to a mechanical force generated in particular by a hydraulic pump that pumps the mobile phase usually from an upstream connection of the column to a downstream connection of the column.
  • a relatively high-pressure drop is generated across the column.
  • the mobile phase with the separated compounds exits the column and passes through a detector, which registers and/or identifies the molecules, for example by spectrophotometric absorbance measurements.
  • a two-dimensional plot of the detector measurements against elution time or volume known as a chromatogram, may be made, and from the chromatogram the compounds may be identified.
  • the chromatogram displays a separate curve feature also designated as a "peak".
  • Efficient separation of the compounds by the column is advantageous because it provides for measurements yielding well defined peaks having sharp maxima inflection points and narrow base widths, allowing excellent resolution and reliable identification and quantitation of the mixture constituents. Broad peaks, caused by poor column performance, so called “Internal Band Broadening” or poor system performance, so called “External Band Broadening” are undesirable as they may allow minor components of the mixture to be masked by major components and go unidentified.
  • sample introduction is provided by fluidically decoupling a sampling volume (such as a sample loop) from a high-pressure path between the chromatographic pump and the chromatographic column.
  • a sampling volume such as a sample loop
  • the sampling volume is fluidically coupled to the high-pressure path for introducing the fluidic sample into the mobile phase driven by the chromatographic pump through the chromatographic column.
  • Such fluidic coupling and decoupling to and from the high-pressure path can cause pressure perturbations which may affect not only the chromatographic measurement (for example by leading to noise into the chromatogram) but also lifetime of certain components in the flow path, in particular the chromatographic column.
  • make-before-break when switching the sampling volume into the high-pressure path between pump and column, the fluidic coupling between pump and column is maintained during switching of the sampling volume, for example by providing extended stator grooves in a rotational valve, as for example disclosed in US8047060B2.
  • make-before-break involves a switching state wherein a fluidic coupling between pump and column is maintained while already the sampling volume is switched between pump and column, so that at least for a short period of time there is a “parallel connection” of the sampling volume with a “shortcut” between the pump and column.
  • a switching unit configured for selectively fluidically coupling a sampling volume, a sampling drive, a mobile phase drive, and a separating device.
  • the mobile phase drive is configured for driving a mobile phase.
  • the separating device is configured for separating a fluidic sample when comprised within the mobile phase.
  • the sampling volume is configured for temporarily storing the fluidic sample, and the sampling drive is configured for moving fluid.
  • the switching unit is configured for fluidically coupling the sampling volume and the sampling drive, for moving the fluidic sample into the sampling volume.
  • the switching unit is configured for fluidically coupling the sampling volume between the sampling drive and the separating device, while the mobile phase drive is fluidically decoupled from the separating device.
  • the switching unit is configured for fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing at least an amount of the fluidic sample stored in the sampling volume into the mobile phase for fluid separation by the separating device.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive during switching from the sample load configuration to the decouple configuration, and during switching from the decouple configuration to the sample introduction configuration. This allows maintaining a fluidic coupling of the separating device with at least one “upstream unit” such as the mobile phase drive, the sampling drive, the sampling volume.
  • the flow to the separating device can be always maintained and may be controlled to provide a flow towards the separating device (for example “actively” by operation of the mobile phase drive, by operation of the sampling drive, and/or “passively” by applying a pressure to the sampling path exceeding a pressure of the mobile phase between the switching unit and the separating device).
  • the switching unit may allow a “make before break” switching by providing a continuous fluidic coupling of and to the separating device in plural (preferably successive) switching states.
  • embodiment of the present invention allow avoiding a pressure decrease at the separating device by maintaining fluidic coupling during successive switching states and by avoiding a fluidic cut off of the separating device (which may cause bad performance and/or reduced column lifetime of the separating device in particular of chromatographic columns.
  • the switching unit in the sample load configuration, is further configured for fluidically coupling the mobile phase drive with the separating device. This allows to provide a flow of the mobile phase from the mobile phase drive to and through the separating device independent of and parallel to the loading of the fluidic sample into the sampling volume.
  • the sampling drive in the sample load configuration, is configured for pressurising or depressurising the fluidic sample in the sampling volume. This allows adjusting the pressure condition of the fluidic sample, for example by pressurising the fluidic sample to a value of pressure corresponding to a value of pressure of the mobile phase or, the other way around, by depressurising the fluidic sample e.g. from a value of pressure in the range of a pressure of the mobile phase to a lower pressure required for loading the fluidic sample, such as ambient pressure.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive during switching between the sample load configuration, the decouple configuration, and the sample introduction configuration.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive in each of the sample load configuration, the decouple configuration, and the sample introduction configuration.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive in each of the sample load configuration, the decouple configuration, and the sample introduction configuration as well as during switching between the sample load configuration, the decouple configuration, and the sample introduction configuration.
  • the switching unit in a couple configuration, is configured for fluidically coupling the sampling volume between the sampling drive and a coupling point between the mobile phase drive and the separating device.
  • the couple configuration may allow to pressurise the fluidic sample in the sampling volume to a pressure value of the mobile phase. Further, the couple configuration may allow Feed-Injection sample introduction, for example by operation of the sampling drive.
  • Pressurising or compressing the fluidic sample prior to introduction of the fluidic sample into the mobile phase may allow to reduce stress to the separation device as may result from resulting pressure ripples.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive during switching between the sample load configuration and the couple configuration.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive during switching between the couple configuration and the sample introduction configuration.
  • the sample introduction configuration comprises a first flow-through configuration, wherein the switching unit is configured for fluidically coupling the sampling volume between the mobile phase drive and the separating device.
  • the switching unit is configured for fluidically coupling the sampling volume between the mobile phase drive and the separating device.
  • the fluidic sample may be transported as a sample plug with the volume of the fluidic sample being substantially spatially focused and may be abutting on each side to the mobile phase.
  • the sampling drive may be coupled to the sampling volume and fluidically coupled between the mobile phase drive and the separating device, or the sampling drive may be decoupled and not being fluidically coupled between the mobile phase drive and a separating device.
  • the sample introduction configuration comprises a second flow-through configuration, wherein the switching unit is configured for fluidically coupling the sampling drive together with the sampling volume between the mobile phase drive and the separating device.
  • the sampling drive and the sampling volume coupled in a serial coupling between the mobile phase drive and the separating device.
  • the sample introduction configuration comprises a Feed-Injection configuration, wherein the switching unit is configured for fluidically coupling the sampling drive together with the sampling volume to a coupling point between the mobile phase drive and the separating device for combining into the coupling point a flow from the sampling drive through the sampling volume with a flow of the mobile phase from the mobile phase drive.
  • a Feed-Injection configuration may be as for example described in US2017343520A1 by the same applicant.
  • the Feed-Injection configuration may correspond to the couple configuration with the difference that the sampling drive can be operated for sample introduction in the Feed-Injection configuration.
  • Embodiments of the present invention provide a switching unit allowing selectively for both sample introduction types, Feed-Injection and flow-through configuration, with the same switching unit, thus allowing a user to select the appropriate sample introduction type for a specific application.
  • a sample dispatcher for a fluid separation apparatus comprises a mobile phase drive, configured for driving a mobile phase, and a separating device configured for separating a fluidic sample when comprised within the mobile phase.
  • the sample dispatcher comprises a sampling volume configured for temporarily storing the fluidic sample, a sampling drive configured for moving fluid, and a switching unit according to any one of the aforedescribed embodiments for selectively fluidically coupling the sampling volume, the sampling drive, the mobile phase drive, and the separating device.
  • the sampling volume comprises at least one of a group of: a sample loop, a sample volume, a trap volume, a trap column, a fluid reservoir, a capillary, a tube, a microfluidic channel structure. While the main functionality of the sample volume is to at least temporarily store fluidic sample, the sample volume may in addition have further capabilities e.g. for sample treatment.
  • the sample dispatcher comprises a sample aspirating unit configured for receiving the fluidic sample.
  • the sample dispatcher comprises a sample aspirating unit configured for receiving the fluidic sample
  • the sample aspirating unit comprises a needle and a needle seat
  • the needle in an open position of the sample aspirating unit the needle is configured to be separated from the needle seat in order to receive the fluidic sample, and in a closed position of the sample aspirating unit the needle is configured to be fluidically sealingly coupled with the needle seat.
  • the needle allows to introduce fluidic sample into the sampling path, e.g. by aspirating such fluidic sample from a vessel, a vial, a conduit providing such fluidic sample e.g. in the sense of an online sampling, or the like.
  • the sample dispatcher comprises a retaining unit configured for receiving and retaining from the sampling volume at least a portion of the fluidic sample stored in the sampling volume, wherein the retaining unit comprises different retention characteristics for different components of the fluidic sample, preferably wherein the retaining unit comprises at least one of a group of: one or more chromatographic columns, preferably at least one of a trapping column, a HILIC column, a guard column, an SPE column, one or more coated capillaries, one or more filters preferably one or more filter frits, wherein in case of plural chromatographic columns and/or coated capillaries at least two of the chromatographic columns and/or coated capillaries having a different chromatographic separation mechanism.
  • the retaining unit can be a single unit comprising only one dedicated retaining property.
  • the retaining unit may comprise plural units, which may be housed individually or combined, preferably at least some of the plural units having different retaining properties, e.g. different retention characteristics for different components. Such plural units may be arranged in parallel or in a serial manner.
  • the switching unit comprises one or more valves, preferably at least one: a shear valve, a rotary valve comprising a rotor and a stator configured for being rotatably moved with respect to each other, a translatory valve comprising a first and a second member configured for being moved with respect to each other by a translatory movement.
  • Typical rotational valves may comprise a rotor and a stator configured for providing a rotational movement with respect to each other in order to switch the valve between different positions.
  • Each of the rotor and the stator, or both, may comprise one or more ports for fluidically coupling external elements to the valve, one or more static grooves configured for providing a fluidic connection between ports, wherein the static grooves will remain static when providing a rotational movement between rotor and stator, and one or more (dynamic) grooves configured for providing a fluidic connection between ports, wherein the (dynamic) grooves can be moved relative to the ports when providing a rotational movement between rotor and stator.
  • the sampling drive comprises at least one of: a metering device configured for metering the fluidic sample, a pump comprising a piston movable within a piston chamber for moving the fluidic sample, a syringe pump, a reciprocating pump.
  • the metering device is preferably configured for precisely metering a desired fluid volume.
  • the metering device may comprise a syringe, a pump, a flow source, a proportioning valve with a pump, or any other adequate facility for metering a desired fluid volume as known in the art.
  • the sampling drive is coupled in series with the sampling volume.
  • a control unit configured to control operation of the sample dispatcher, preferably at least one of operation of the sampling drive and switching of the switching unit.
  • a fluid separation apparatus comprising a mobile phase drive, configured for driving a mobile phase, and a separating device configured for separating a portion of a fluidic sample when comprised within the mobile phase.
  • the fluid separation apparatus further comprises a sample dispatcher, according to any one of the aforedescribed embodiments, configured for dispatching at least a portion of the fluidic sample to the fluid separation apparatus.
  • a method of sample separation comprising: fluidically coupling a mobile phase drive with a separating device for driving a mobile phase through the separating device; in a sample load configuration, loading a fluidic sample into a sampling volume; in a decouple configuration, fluidically coupling one end of the sampling volume to the separating device while the other end of the sampling volume is substantially blocked (e.g. disabling flow), and fluidically decoupling the mobile phase drive from the separating device; and in a sample introduction configuration, fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing at least an amount of the fluidic sample stored in the sampling volume into the mobile phase for fluid separation by the separating device.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive during switching from the sample load configuration to the decouple configuration, and during switching from the decouple configuration to the sample introduction configuration.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive during switching between the sample load configuration, the decouple configuration, and the sample introduction configuration
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive in each of the sample load configuration, the decouple configuration, and the sample introduction configuration.
  • the separating device is fluidically coupled with at least one of the mobile phase drive and the sampling drive in each of the sample load configuration, the decouple configuration, and the sample introduction configuration as well as during switching between the sample load configuration, the decouple configuration, and the sample introduction configuration.
  • loading the fluidic sample into the sampling volume comprises fluidically coupling the sampling volume with a sampling drive and operating the sampling drive for moving the fluidic sample into the sampling volume, preferably while a mobile phase drive is driving a mobile phase through a separating device.
  • the mobile phase drive while loading the fluidic sample into the sampling volume, the mobile phase drive is fluidically coupled with the separating device.
  • One embodiment comprises, fluidically coupling one end of the sampling volume to the separating device while the other end of the sampling volume is substantially blocked comprises coupling one end of a sampling drive to the other end of the sampling volume and blocking the other end of the sampling device.
  • One embodiment comprises, after loading the fluidic sample into the sampling volume, operating the sampling drive for pressurising the fluidic sample in the sampling volume, preferably before fluidically coupling the sampling volume between the sampling drive and the separating device and fluidically decoupling the mobile phase drive from the separating device, and/or before fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing the amount of the fluidic sample stored in the sampling volume into the mobile phase for fluid separation by the separating device.
  • One embodiment comprises, after introducing the amount of the fluidic sample stored in the sampling volume into the mobile phase for fluid separation by the separating device, fluidically coupling the sampling volume with the sampling drive and operating the sampling drive for depressurising the fluidic sample in the sampling volume, preferably after fluidically decoupling the sampling volume and the sampling drive from the mobile phase drive and the separating device, and preferably while the mobile phase drive is fluidically coupled to the separating device.
  • One embodiment corresponding to the aforedescribed couple configuration comprises, after loading the fluidic sample into the sampling volume, fluidically coupling the sampling volume between the sampling drive and the separating device, and fluidically coupling the mobile phase drive with the separating device.
  • One embodiment corresponding to the aforedescribed first flow-through comprises, during introducing the amount of fluidic sample into the mobile phase, fluidically coupling the sampling volume between the mobile phase drive and the separating device.
  • One embodiment corresponding to the aforedescribed second flow-through configuration comprises, during introducing the amount of fluidic sample into the mobile phase, fluidically coupling the sampling drive together with the sampling volume (preferably in a serial connection) between the mobile phase drive and the separating device.
  • One embodiment corresponding to the aforedescribed Feed-Injection configuration comprises, during introducing the amount of fluidic sample into the mobile phase, fluidically coupling the sampling drive together with the sampling volume to a coupling point between the mobile phase drive and the separating device, and combining into the coupling point a flow from the sampling drive through the sampling volume with a flow of the mobile phase from the mobile phase drive.
  • a method of sample separation comprising: fluidically coupling a mobile phase drive with a separating device for driving a mobile phase through the separating device, loading a fluidic sample into a sampling volume, fluidically coupling the sampling volume between a sampling drive and a coupling point between the mobile phase drive and the separating device, so that a pressure of the mobile phase at the coupling point pressurizes the fluidic sample, and fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing at least an amount of the pressurised fluidic sample into the mobile phase for fluid separation by the separating device.
  • This allows pressurising the fluidic sample without requiring an additional pump, drive (such as the sampling drive), or other pressure source, but only by fluidically coupling to the high-pressure path of the mobile phase.
  • One embodiment comprises, after pressurising the fluidic sample and before introducing the fluidic sample into the mobile phase, fluidically coupling the sampling volume between the sampling drive and a separating device.
  • One embodiment comprises, fluidically decoupling the mobile phase drive from the separating device.
  • One embodiment comprises operating the sampling drive to further pressurise the fluidic sample.
  • the fluidic sample can be pressurised beyond the pressure of the mobile phase at the coupling point, which may be useful for compensating an expected or assumed pressure drop when introducing the fluidic sample into the mobile phase.
  • fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing the amount of the pressurised fluidic sample into the mobile phase comprises (preferably corresponding to the first flow-through configuration) fluidically coupling the sampling volume between the mobile phase drive and the separating device.
  • fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing the amount of the pressurised fluidic sample into the mobile phase comprises (preferably corresponding to the second flow-through configuration) fluidically coupling the sampling drive together with the sampling volume (preferably in a serial connection) between the mobile phase drive and the separating device.
  • fluidically coupling the mobile phase drive, the sampling volume, and the separating device for introducing the amount of the pressurised fluidic sample into the mobile phase comprises (preferably corresponding to the Feed-Injection configuration) operating the sampling drive to provide a flow through the sampling volume, and combining into the coupling point the flow from the sampling drive through the sampling volume with a flow of the mobile phase from the mobile phase drive for fluid separation of the fluidic sample by the separating device.
  • a control unit is configured to control operation of the sample dispatcher, preferably at least one of operation of the sampling drive and switching of the switching unit.
  • Embodiments of the present invention might be embodied based on most conventionally available HPLC systems, such as the Agilent 1220, 1260 and 1290 Infinity LC Series (provided by the applicant Agilent Technologies).
  • One embodiment of an HPLC system comprises a pumping apparatus having a piston for reciprocation in a pump working chamber to compress liquid in the pump working chamber to a high pressure at which compressibility of the liquid becomes noticeable.
  • One embodiment of an HPLC system comprises two pumping apparatuses coupled either in a serial or parallel manner.
  • serial manner as disclosed in EP 309598 A1 .
  • an outlet of the first pumping apparatus is coupled to an inlet of the second pumping apparatus, and an outlet of the second pumping apparatus provides an outlet of the pump.
  • parallel manner an inlet of the first pumping apparatus is coupled to an inlet of the second pumping apparatus, and an outlet of the first pumping apparatus is coupled to an outlet of the second pumping apparatus, thus providing an outlet of the pump.
  • a liquid outlet of the first pumping apparatus is phase shifted, preferably essentially by 180 degrees, with respect to a liquid outlet of the second pumping apparatus, so that only one pumping apparatus is supplying into the system while the other is intaking liquid (e.g. from the supply), thus allowing to provide a continuous flow at the output.
  • both pumping apparatuses might be operated in parallel (i.e. concurrently), at least during certain transitional phases e.g. to provide a smooth(er) transition of the pumping cycles between the pumping apparatuses.
  • the phase shifting might be varied in order to compensate pulsation in the flow of liquid as resulting from the compressibility of the liquid. It is also known to use three piston pumps having about 120 degrees phase shift. Also other types of pumps are known and operable in conjunction with the present invention.
  • the separating device preferably comprises a chromatographic column providing the stationary phase.
  • the column might be a glass, metal, ceramic or a composite material tube (e.g. with a diameter from 50 pm to 5 mm and a length of 1 cm to 1 m) or a microfluidic column (as disclosed e.g. in EP 1577012 A1 or the Agilent 1200 Series HPLC-Chip/MS System provided by the applicant Agilent Technologies).
  • the individual components are retained by the stationary phase differently and separate from each other while they are propagating at different speeds through the column with the eluent. At the end of the column they elute at least partly separated from each other.
  • the stationary phase or adsorbent in column chromatography usually is a solid material.
  • the most common stationary phase for column chromatography is silica gel, followed by alumina. Cellulose powder has often been used in the past. Also possible are ion exchange chromatography, reversed- phase chromatography (RP), affinity chromatography or expanded bed adsorption (EBA).
  • RP reversed- phase chromatography
  • EBA expanded bed adsorption
  • the stationary phases are usually finely ground powders or gels and/or are microporous for an increased surface, which can be especially chemically modified, though in EBA a fluidized bed is used.
  • the mobile phase can be either a pure solvent or a mixture of different solvents. It can also contain additives, i.e. be a solution of the said additives in a solvent or a mixture of solvents. It can be chosen e.g. to adjust the retention of the compounds of interest and/or the amount of mobile phase to run the chromatography.
  • the mobile phase can also be chosen so that the different compounds can be separated effectively.
  • the mobile phase might comprise an organic solvent like e.g. methanol or acetonitrile, often diluted with water. For gradient operation water and organic solvent is delivered in separate containers, from which the gradient pump delivers a programmed blend to the system.
  • Other commonly used solvents may be isopropanol, THF, hexane, ethanol and/or any combination thereof or any combination of these with aforementioned solvents.
  • the sample fluid might comprise any type of process liquid, natural sample like juice, body fluids like plasma or it may be the result of a reaction like from a fermentation broth.
  • the fluid is preferably a liquid but may also be or comprise a gas and/or a supercritical fluid (as e.g. used in supercritical fluid chromatography - SFC - as disclosed e.g. in US 4,982,597 A).
  • a supercritical fluid as e.g. used in supercritical fluid chromatography - SFC - as disclosed e.g. in US 4,982,597 A.
  • the pressure in the mobile phase might range from 2-200 MPa (20 to 2000 bar), in particular 10-150 MPa (100 to 1500 bar), and more particular 50-130 MPa (500 to 1300 bar).
  • the FIPLC system might further comprise a detector for detecting separated compounds of the sample fluid, a fractionating unit for outputting separated compounds of the sample fluid, or any combination thereof. Further details of FIPLC system are disclosed with respect to the aforementioned Agilent FIPLC series, provided by the applicant Agilent Technologies.
  • Embodiments of the invention can be partly or entirely embodied or supported by one or more suitable software programs or products, which can be stored on or otherwise provided by any kind of data carrier, and which might be executed in or by any suitable data processing unit.
  • Software programs or routines can be preferably applied in or by the control unit, e.g. a data processing system such as a computer, preferably for executing any of the methods described herein.
  • fluidic sample may particularly denote any liquid and/or gaseous medium, optionally including also solid particles, which is to be analyzed.
  • a fluidic sample may comprise a plurality of fractions of molecules or particles which shall be separated, for instance biomolecules such as proteins. Since separation of a fluidic sample into fractions involves a certain separation criterion (such as mass, volume, chemical properties, etc.) according to which a separation is carried out, each separated fraction may be further separated by another separation criterion (such as mass, volume, chemical properties, etc.) or finer separated by the first separation criterion, thereby splitting up or separating a separate fraction into a plurality of sub-fractions.
  • separation criterion such as mass, volume, chemical properties, etc.
  • the term “fraction” may particularly denote such a group of molecules or particles of a fluidic sample which have one or more certain properties of the group of: mass, charge, volume, chemical or physical properties or interaction, etc.in common according to which the separation has been carried out. However, molecules or particles relating to one fraction can still have some degree of heterogeneity, i.e. can be further separated in accordance with another separation criterion. As well the term "fraction” may denote a portion of a solvent containing the aforementioned group of molecules.
  • downstream may particularly denote that a fluidic member located downstream compared to another fluidic member will only be brought in interaction with a fluidic sample after interaction with the other fluidic member (hence being arranged upstream). Therefore, the terms “downstream” and “upstream” relate to a flowing direction of the fluidic sample. The terms “downstream” and “upstream” may also relate to a preferred direction of the fluid flow between the two members being in downstream-upstream relation.
  • sample separation apparatus may particularly denote any apparatus which is capable of separating different fractions of a fluidic sample by applying a certain separation technique.
  • two separation apparatus may be provided in such a sample separation apparatus when being configured for a two-dimensional separation. This means that the sample is first separated in accordance with a first separation criterion, and at least one or some of the fractions resulting from the first separation are subsequently separated in accordance with a second, different, separation criterion or more finely separated in accordance with the first separation criterion.
  • separation unit may particularly denote a fluidic member through which a fluidic sample is transferred, and which is configured so that, upon conducting the fluidic sample through the separation unit, the fluidic sample will be separated into different groups of molecules or particles (called fractions or sub-fractions, respectively).
  • An example for a separation unit is a liquid chromatography column which is capable of trapping or retaining and selectively releasing different fractions of the fluidic sample.
  • fluid drive may particularly denote any kind of pump which is configured for forcing a flow of mobile phase and/or a fluidic sample along a fluidic path.
  • a corresponding liquid supply system may be configured for delivery of a single liquid or of two or more liquids in controlled proportions and for supplying a resultant mixture as a mobile phase.
  • the first fluid drive can be configured to drive the fluidic sample, usually mixed with, or injected into a flow of a mobile phase (solvent composition), through the first- dimension separation apparatus
  • the second fluid drive can be configured for driving the fluidic sample fractions, usually mixed with a further mobile phase (solvent composition), after treatment (e.g. elution) by the first-dimension separation unit through the second-dimension separation apparatus.
  • the term “flow coupler” or “coupling point” may particularly denote a fluidic component which is capable of unifying flow components from two fluid inlet terminals into one common fluid outlet terminal.
  • a bifurcated flow path may be provided in which two streams of fluids flow towards a bifurcation point are unified to flow together through the fluid outlet terminal.
  • fluid may flow from any source terminal to any destination terminal depending on actual pressure conditions.
  • the flow coupler may act as a flow combiner for combining flow streams from the two fluid inlet terminals further flowing to the fluid outlet terminal.
  • the flow coupler may provide for a permanent (or for a selective) fluid communication between the respective fluid terminals and connected conduits, thereby allowing for a pressure equilibration between these conduits.
  • the flow coupler may also act as a flow splitter.
  • a respective coupling point may be configured as one of the group consisting of a fluidic T-piece, a fluidic Y-piece, a fluidic X-piece, microfluidic junction, a group of at least 3 ports of a rotary valve, connectable together in at least one of configurations of the said rotary valve and a multi-entry port of a rotary valve.
  • valve or “fluidic valve” may particularly denote a fluidic component which has fluidic interfaces, wherein upon switching the fluidic valve selective ones of the fluidic interfaces may be selectively coupled to one another so as to allow fluid to flow along a corresponding fluidic path, or may be decoupled from one another, thereby disabling fluid communication.
  • buffer or “buffering” may particularly be understood as temporarily storing. Accordingly, the term “buffering fluid” is preferably understood as temporarily storing an amount of fluid, which may later be fully or partly retrieved from such unit buffering the fluid.
  • the term “loop” may particularly be understood as a fluid conduit allowing to temporarily store an amount of fluid, which may later be fully or partly retrieved from the loop.
  • such loop has an elongation along the flow direction of the fluid and a limited mixing characteristic (e.g. resulting from dispersion), so that a spatial variation in composition in the fluid will be at least substantially maintained along the elongation of the loop.
  • sample loop may be understood as a loop configured to temporarily store an amount of sample fluid.
  • a sample loop is preferably configured to at least substantially maintain a spatial variation in the sample fluid (along the flow direction of the sample), as e.g. resulting from a previous chromatographic separation of the sample fluid, during temporarily storing of such sample fluid.
  • the term “retain”, “retaining”, or similar, in particular in context with “unit”, may particularly be understood as providing a surface (e.g. a coating) and/or a stationary phase configured for interacting with a fluid in the sense of having a desired retention characteristics with one or more components contained in the fluid.
  • desired retention characteristics shall be understood as an intentionally applied retention, i.e. a retention beyond an unintentional side-effect.
  • the term “retaining unit” may be understood as a unit in a fluidic path being configured for interacting with a sample fluid for providing a desired retention characteristic for one or more components contained in the sample fluid.
  • fluidically coupling may particularly be understood as providing a fluidic connection at least during a desired time interval.
  • Such fluidic connection may not be permanent but allows a (passive and/or active) transport of fluid between the components fluidically coupled to each other at least during such desired time interval.
  • fluidically coupling may involve active and/or passive components, such as one or more fluid conduits, switching elements (such as valves), et cetera.
  • the fluid separation apparatus may be configured to drive the mobile phase through the system by means of a high pressure, particularly of at least 400 bar, more particularly of at least 1000 bar.
  • FIG. 1 illustrates a liquid chromatography system according to an exemplary embodiment.
  • Figures 2 illustrate schematically an exemplary embodiment of the sample dispatcher 40.
  • Figures 3 illustrates the fluidic coupling, e.g. according to the embodiment of Figures 2, in an overview schematic representation.
  • Figures 4 illustrate another exemplary embodiment of the switching unit 200.
  • Fig. 1 depicts a general schematic of a liquid separation system 10.
  • a mobile phase drive 20 (such as a pump) receives a mobile phase from a solvent supply 25, typically via a degasser 27, which degases the mobile phase and thus reduces the amount of dissolved gases in it.
  • the mobile phase drive 20 drives the mobile phase through a separating device 30 (such as a chromatographic column).
  • a sample dispatcher 40 (also referred to as sample introduction apparatus, sample injector, etc.) is provided between the mobile phase drive 20 and the separating device 30 in order to subject or add (often referred to as sample introduction) portions of one or more sample fluids into the flow of a mobile phase (denoted by reference numeral 200, see also Fig. 2).
  • the separating device 30 is adapted for separating compounds of the sample fluid, e.g. a liquid.
  • a detector 50 is provided for detecting separated compounds of the sample fluid.
  • a fractionating unit 60 can be provided for outputting separated compounds of sample fluid.
  • the separating device 30 may comprise a stationary phase configured for separating compounds of the sample fluid.
  • the separating device 30 may be based on a different separation principle (e.g. field flow fractionation).
  • the mobile phase can be comprised of one solvent only, it may also be mixed of plurality of solvents. Such mixing might be a low pressure mixing and provided upstream of the mobile phase drive 20, so that the mobile phase drive 20 already receives and pumps the mixed solvents as the mobile phase.
  • the mobile phase drive 20 might be comprised of plural individual pumping units, with plural of the pumping units each receiving and pumping a different solvent or mixture, 3so that the mixing of the mobile phase (as received by the separating device 30) occurs at high pressure und downstream of the mobile phase drive 20 (or as part thereof).
  • the composition (mixture) of the mobile phase may be kept constant over time, the so-called isocratic mode, or varied over time, the so-called gradient mode.
  • a data processing unit 70 which can be a conventional PC or workstation, might be coupled (as indicated by the dotted arrows) to one or more of the devices in the liquid separation system 10 in order to receive information and/or control operation.
  • the data processing unit 70 might control operation of the mobile phase drive 20 (e.g. setting control parameters) and receive therefrom information regarding the actual working conditions (such as output pressure, flow rate, etc. at an outlet of the pump).
  • the data processing unit 70 might also control operation of the solvent supply 25 (e.g. monitoring the level or amount of the solvent available) and/or the degasser 27 (e.g.
  • the data processing unit 70 might further control operation of the sample dispatcher 40 (e.g. controlling sample introduction or synchronization of the sample introduction with operating conditions of the mobile phase drive 20).
  • the separating device 30 might also be controlled by the data processing unit 70 (e.g. selecting a specific flow path or column, setting operation temperature, etc.), and send - in return - information (e.g. operating conditions) to the data processing unit 70.
  • the detector 50 might be controlled by the data processing unit 70 (e.g. with respect to spectral or wavelength settings, setting time constants, start/stop data acquisition), and send information (e.g.
  • the data processing unit 70 might also control operation of the fractionating unit 60 (e.g. in conjunction with data received from the detector 50) and provides data back.
  • the data processing unit 70 might also process the data received from the system or its part and evaluate it in order to represent it in adequate form prepared for further interpretation.
  • Figures 2 illustrate schematically an exemplary embodiment of the sample dispatcher 40, which may be part of the liquid separation system 10.
  • the representation of Figure 2 shall only depict such parts and components required for explaining function and operation of the sample dispatcher 40.
  • Figures 2A-2D illustrate operation of the sample dispatcher 40, while Figure 2E details a preferred embodiment of rotor and stator configuration.
  • the sample dispatcher 40 (as generally shown in Figure 1 ) is provided by a switching unit 200 for selectively fluidically coupling the mobile phase drive 20, the separating device 30, and a sampling path 210.
  • the switching unit 200 may be embodied by a rotary valve, as best visible in the separated representation of Figure 2E, having a stator 220 and a rotor 225.
  • a rotary valve as well known in the art, the stator 220 and the rotor 225 can be rotated with respect to each other, with typically the stator 220 being held in place while the rotor 225 can be rotated, for example as driven by an actuator and/or motor (not shown or further detailed herein).
  • the stator 220 has four ports 1 -4, each allowing to fluidically couple with a respective component (e.g. as illustrated in Figures 2A-D).
  • a stator groove 230 extends from port 3 in the direction towards port 2.
  • port 1 is located at -45°
  • port 2 at +-180°
  • port 3 at 75°
  • port 4 at 30°
  • stator groove 230 is extending from about 75°-105°.
  • the rotor 225 in the embodiments of Figures 2 comprises a first groove 240 (extending about 75°) and a second groove 245 (extending about 105°).
  • the sampling path 210 is comprised by a sampling drive 250, a sampling volume 255, and a sampling unit 260.
  • the sampling unit 260 comprises a needle 263 and a seat 265.
  • the needle 263 can be removed from the seat 265, for example as schematically depicted (dotted lines) on the left- hand side of Figure 2A, for being immersed into a sampling container 270 (e.g. a sample vial) containing a fluidic sample (such as a sample liquid).
  • a fluid tight connection between needle 263 and seat 265 can be provided, thus providing a fluid tight sampling unit 260 within the sampling path 210.
  • the needle 263 is removed from the seat 265 and immersed into the container 270 (dotted line).
  • fluidic sample from the container 270 can be aspirated via the needle 263 and transported into the sampling volume 255, as well known in the art.
  • the needle 263 can then be returned back and situated into the seat 265 (solid line).
  • the sampling path 210 is coupled on one side to port 1 and on the opposing side to port 2 of the stator 220, so that the sampling drive 250 is an integral part of the sampling path 210.
  • the sampling drive 250 may also become decoupled from the sampling path 210, e.g. during certain switching configurations, for example as described and shown in WO201 4199198A1 by the same applicant, preferably to avoid switching the sampling drive 250 between the mobile phase drive 20 and the separating device 30 for example during injection of the fluidic sample into the mobile phase.
  • the sampling path 210 may further comprise a sensor 275, such as a pressure sensor, which may be located, as shown in Figures 2, between the sampling drive 250 and port 1 , or at any adequate location either within the sampling path 210 or fluidically coupled thereto.
  • a sensor 275 such as a pressure sensor, which may be located, as shown in Figures 2, between the sampling drive 250 and port 1 , or at any adequate location either within the sampling path 210 or fluidically coupled thereto.
  • Figure 2A shows a so-called sample load configuration, allowing on one hand loading fluidic sample into the sampling volume 255, while at the same time the mobile phase drive 20 is coupled via the first groove 240 to the separating device 30.
  • the fluidic path between the mobile phase drive 20 and the separating device 30 represents a high-pressure (flow) path, typically at a pressure in the range of several hundred bars up to 2000 bar and even beyond.
  • the sampling path 210 - at least during loading of the fluidic sample - is typically at about ambient pressure.
  • the fluidic sample may be pressurised (in the configuration shown in Figure 2A) by operation of the sampling drive 250.
  • the sampling drive 250 As one side of the sampling drive 250 is coupled to port 1 , which in the configuration of Figure 2A is blocked (i.e.
  • port 1 is not fluidically coupled with any other port or component, thus representing a blockage
  • the other end of the sampling path 210 is blocked (as port 2 is only coupled with the second groove 245 which, however, is not fluidically coupled with any other port or component, thus also representing a blockage)
  • operation of the sampling drive 250 for example by moving a piston in the direction of arrow 280, compresses the sampling path 210 and thus the fluidic sample within the sampling volume 255.
  • Pressurising the fluidic sample may be controlled for example by usage of the sensor 275 allowing to determine a current value of the pressure in the sampling path 210.
  • pressurisation may be executed based on knowledge of the actual conditions in the sampling path 210 (for example knowledge about the liquid content within the sampling path 210, in particular volumes and characteristics of such liquid content, and/or elasticity of the sampling path, et cetera), and/or historical data (e.g. effects of previous pressurising for example resulting in pressure ripples when introducing the fluidic sample into the high-pressure path of the mobile phase, as will be explained later), and/or simulation, et cetera.
  • the fluidic sample may be pressurised to the pressure of the mobile phase (in the high-pressure path between the mobile phase drive 20 and the separation device 30) or within a certain range below are beyond such pressure. Pressurising the fluidic sample to a pressure value higher than a pressure of the mobile phase may be useful to compensate for an (e.g. expected) pressure drop when introducing the fluidic sample into the mobile phase.
  • Such over-pressurising may be done iteratively by, in a first cycle, pressurising the fluidic sample to a first pressure value higher than the pressure of the mobile phase and determining a pressure ripple when introducing the fluidic sample into the mobile phase, and in a successive cycle varying (with respect to the first pressure value) the pressure value for over-pressurising of the fluidic sample in order to avoid or at least reduce such pressure ripple.
  • this may be executed iteratively and adaptively in order to minimise the resulting pressure ripple resulting from introducing the fluidic sample into the mobile phase.
  • Figure 2B shows the switching unit 200 in a “couple configuration”.
  • Such couple configuration can be assumed, when starting from the sample load configuration of Figure 2A and rotating rotor 225 in anticlockwise direction.
  • the stator groove 230 is coupling between the first groove 240 and the second groove 245, so that the first groove 240, the stator groove 230 and the second groove 245 represent a common “enlarged” groove.
  • the separating device 30 remains fluidically coupled with the mobile phase drive 20 during switching from the sample load configuration (of Fig. 2A) to the couple configuration (of Fig. 2B).
  • the “enlarged” groove (provided by the first groove 240, the stator groove 230 and the second groove 245) fluidically couples ports 2-4 together, so that ports 2-3 can be considered as a single coupling point.
  • the sampling path 210 couples with one side (namely the side coupled to port 2) in the high-pressure path between the mobile phase drive 20 and the separating device 30.
  • the pressure condition at the coupling point (ports 2-4) is the same for the coupling end of the sampling path 210 and for the mobile phase in the high-pressure path.
  • the pressure in the sampling path 210 is substantially the same as at the coupling point, there will be no flow from the sampling path 210 into the high-pressure path, or the other way around, and also there will be no change in the pressure of the sampling path 210.
  • the sampling path 210 In case the pressure in the sampling path 210 is smaller than at the coupling point, and given that the sampling path 210 at port 1 is blocked, the sampling path 210 will be pressurised (from the high-pressure path) until an equilibrium is reached (typically when the sampling path 210 has substantially the pressure of the high-pressure path at the coupling point). Accordingly, when the pressure in the sampling path 210 is higher than at the coupling point, this will result in a flow from the sampling path 210 into the high-pressure path.
  • the couple configuration of Figure 2B represents a “Feed-Injection” position or configuration as for example described in the aforementioned US2017343520A1 by the same applicant.
  • Such Feed-Injection position allows introducing fluidic sample from the sampling volume into the mobile phase for sample separation by the separating device 30, by combining a flow from the sampling path 210 with a flow of the mobile phase from the mobile phase drive 20.
  • Such fluidic sample introduction can be operated and controlled in particular dependent on the pressure condition at the coupling point (ports 2-4) and the pressure in the sampling path 210.
  • Controlling the pressure in the sampling path 210 thus allows controlling the introduction of the fluidic sample into the mobile phase, in particular with respect to a volume of fluidic sample introduced over time.
  • the sampling drive 250 to rapidly pressurise the sampling path 210 allows to rapidly introduce a certain volume of fluidic sample into the mobile phase (for sample separation by the separating device 30), for example in the sense of a so-called sample plug (i.e. during sample introduction, the introduced liquid volume flown from the coupling point towards the separating device 30 is substantially, e.g. either fully or to a higher extent, provided by the fluidic sample).
  • sample plug introduction corresponds to the so-called “flow-through injection”, as described e.g.
  • the sampling drive 250 may be operated in away that the flow from the sampling point (towards the separating device 30) is a combined flow with substantial contributions of liquid content from the sampling path 210 and the mobile phase provided from the mobile phase drive 20.
  • the couple configuration shown in Figure 2B may be a dedicated position to be assumed by the switching unit 200, e.g. for providing a Feed-Injection sample introduction as aforedescribed.
  • the couple configuration of Figure 2B may only represent an intermediate position, for example when rotating the rotor 225 from the sample load configuration of Figure 2A towards a “decouple configuration” depicted in Figure 2C (illustrated below).
  • the immediate position may merely represent a configuration of the switching unit 200 as resulting from rotating the rotor 225 with respect to the stator 220 and may thus not have a desired functionality.
  • the sampling path 210 is fluidically coupled via ports 2 and 3 to the separating device 30. Accordingly, the separating device 30 remains coupled with the sampling path 210 and thus with the sampling drive 250 during switching from the couple configuration (Figure 2B) into the decouple configuration ( Figure 2C).
  • FIG. 2D illustrates a sample introduction configuration corresponding to the so-called “flow-through injection”, as described e.g. in the aforementioned US20160334031 A1 by the same applicant.
  • the sampling volume 255 (comprising the fluidic sample) is now switched between the mobile phase drive 20 and the separating device 30, so that the fluidic sample will be transported and driven by the mobile phase drive 20 through the separating device 30 (for fluidic separation of the fluidic sample by the separating device 30).
  • the first groove 240 is coupling between ports 1 and 4, thus coupling the mobile phase drive 20 to one end of the sampling path 210, while the second groove 245 is coupling between ports 2 and 3, thus coupling the other end of the sampling path 210 to the separating device 30. Accordingly, the separating device 30 remains coupled with the sampling path 210 and thus with the sampling drive 250 during switching from the decouple configuration (Figure 2C) into the injection couple configuration ( Figure 2D).
  • the switching unit 200 represents a so-called “hybrid” switching unit in the sense of selectively allowing both different types of sample introduction, namely flow-through injection and Feed-Injection.
  • flow-through injection or Feed-Injection for introducing the fluidic sample into the mobile phase can be selected or even a sequential combination of both.
  • an amount of the fluidic sample can first be introduced by Feed-Injection and the then remaining amount of the fluidic sample can then/later be introduced by flow-through injection.
  • sample dispatcher 40 (and accordingly the same switching unit 200) can be operated in different modes of operation dependent on the respective application.
  • the same embodiment of the sample dispatcher 40 may in one application be operated to apply flow-through injection for sample introduction, may then be operated in a different application to apply Feed-Injection for sample introduction, and may even be operated in a further application to first apply Feed-Injection for introducing an amount of the fluidic sample and then apply flow-through injection for introducing the remaining portion of the fluidic sample.
  • the exemplary switching unit 200 as illustrated with respect to Figures 2 allows pressurising the fluidic sample contained in the sampling volume.
  • the sampling volume is precompressed, e.g. by operation of the sampling drive 250, before sample introduction (by Feed-Injection and/or flow-through injection), for example in order to pressurise the fluidic sample to a value of pressure in the range of the pressure of the mobile phase (e.g. between the switching unit 200 and the separating device 30).
  • sample introduction by Feed-Injection and/or flow-through injection
  • sample introduction is applied with the fluidic sample being substantially at ambient pressure.
  • pressurising the fluidic sample can be provided by operation of the sampling drive 250 (as explained with respect to Figure 2A) and/or by operating the switching unit 200 into the couple configuration (as explained with respect to Figure 2B) wherein the pressurised mobile phase (as provided by the mobile phase drive 20) can pressurise the sampling path 210 when coupled at the coupling point (ports 2-4 in Figure 2B).
  • the switching unit 200 is operated into the sample load configuration of Figure 2A for loading fluidic sample e.g. from the container 270 into the sampling volume 255.
  • the fluidic sample may then also be precompressed by operation of the sampling drive 250.
  • Sample introduction shall then be applied by flow-through injection, and the sampling unit 200 is operated from the sample load configuration of Figure 2A towards the sample introduction configuration of Figure 2D by rotating the rotor 225 relative to the stator 220.
  • rotation of the rotor 225 will also assume the configurations of Figures 2B and 2C.
  • the rotor 225 shall be operated to assume the configurations of Figures 2B and 2C only in the sense of intermediate configurations, for example by “rotating over” without substantially resting at these intermediate configurations of Figures 2B and 2C.
  • the rotor 225 will assume and rest in the configurations of Figure 2A and Figure 2D, i.e. rotation velocity of the rotor 225 is e.g. zero during given periods of time in the configurations of Figure 2A and Figure 2D
  • the rotor 225 will “rotate over” these intermediate configurations of Figures 2B and 2C e.g. with the rotation velocity at which the rotor 225 is operated.
  • the rotor 225 may stay in each of the configurations of Figure 2A and Figure 2D from about 10 seconds to several minutes, while rotating over of the rotor 225 in the intermediate configurations of Figures 2B and 2C may take only about 10-30 ms (dependent on the operation and applicable rotational velocity of the rotor 225).
  • the rotor 225 (starting from the position of Figure 2A) passes the positions of Figures 2B and 2C as intermediate positions.
  • the flow from the mobile phase drive 20 to the separating device 30 will continue, and the position of Figure 2B will have substantially no influence on the sampling path 210.
  • a certain flow and/or pressurisation will occur - as long as the position of Figure 2B is assumed - dependent on the respective pressure conditions.
  • the pressure of the mobile phase is higher than at the fluidic sample (in the sampling volume 255), a flow of mobile phase from the coupling point into the sampling path 210 will occur and the fluidic sample may be pressurised.
  • the pressure of the mobile phase is lower than at in the sampling path 210, a flow from the sampling path 210 into the mobile phase will occur.
  • the rotor 225 passes - as intermediate position - the decouple configuration of Figure 2C, which substantially corresponds to the previous (intermediate) configuration of Figure 2B, however, with the difference that the mobile phase drive 20 is now decoupled (from both the sampling path 210 and the separating device 30), while the sampling path 210 remains coupled with the separating device 30.
  • the rotor 225 will assume the sample introduction configuration of Figure 2D for introducing the fluidic sample into the mobile phase for separation by the separating device 30.
  • decoupling the mobile phase drive 20 during the intermediate position of Figure 2C may lead to a variation in solvent composition as seen by the separating device 30. This may be compensated by adequately controlling solvent composition in order to balance such composition variation, preferably by adequately modifying solvent composition before and/or after the switching process.
  • the switching unit 200 may be rotated backwards to assume the loading configuration of Figure 2A.
  • a remaining pressure (e.g. beyond ambient pressure as may be applied for a successive sample loading) in the sampling path 210 may be reduced or removed, for example by operation of the sampling drive 250, e.g. by moving the piston of the sampling drive 250 opposite to the arrow 280.
  • Such depressurising may help avoiding undesired pressure effects, e.g. when removing the needle 263 from the seat 265, for example for successive sample loading.
  • FIG. 2A For loading from fluidic sample (e.g. from the container 270) into the sampling volume 255.
  • the fluidic sample (contained in the sampling volume 255) is then preferably precompressed by operation of the sampling drive 250, for example so that the pressure in the sampling volume 255 substantially corresponds to the pressure of the mobile phase.
  • the rotor 225 is then turned into the position of Figure 2B, which represents a Feed-Injection configuration with the sampling path 210 coupling to the coupling point (ports 2-4) in the high-pressure flow path of the mobile phase between the mobile phase drive 20 and the separating unit 30.
  • Controlling the pressure in the sampling path 210 allows combining flow of fluidic sample from the sampling path 210 with a flow of mobile phase from the mobile phase drive 20 towards the separating unit 30 (for chromatographically separating compounds of the fluidic sample contained in the mobile phase).
  • a combined sample introduction applying Feed-Injection as well as flow-through injection is applied.
  • fluidic sample e.g. from the container 270
  • the fluidic sample obtained in the sampling volume 255) is then preferably precompressed by operation of the sampling drive 250, for example so that the pressure in the sampling volume 255 substantially corresponds to the pressure of the mobile phase.
  • the rotor 225 is then turned into the position of Figure 2B, which represents a Feed-Injection configuration with the sampling path 210 coupling to the coupling point (ports 2-4) in the high-pressure flow path of the mobile phase between the mobile phase drive 20 and the separating unit 30.
  • Controlling the pressure in the sampling path 210 preferably by operation of the sampling drive 250, allows combining a flow of fluidic sample from the sampling path 210 with a flow of mobile phase from the mobile phase drive 20 towards the separating unit 30 (for chromatographically separating compounds of the fluidic sample contained in the mobile phase) until a predefined amount of fluidic sample has been introduced into the mobile phase.
  • the rotor 225 may stay into the configuration of Figure 2B, however, with the sampling drive 250 being operated that no further flow from the sampling path 210 is combined with the flow of mobile phase from the mobile phase drive 20. Alternatively to staying in the configuration of Figure 2B, the rotor 225 may be rotated for example returning into the configuration of Figure 2A or for assuming any other suitable configuration.
  • the process of sample introduction applying Feed-Injection may be applied several times in the third mode of operation, each time for introducing a certain amount of fluidic sample into the mobile phase for chromatographic separation.
  • the rotor 225 is then operated to assume the configuration of Figure 2D, as explained above with respect to the first mode of operation. In accordance with the first mode of operation and dependent on the starting position of the rotor 225, the rotor 225 will pass the positions of Figures 2B and/or 2C as intermediate positions.
  • Figures 3 shall illustrate the fluidic coupling of the mobile phase drive 20, the separating device 30, and the sampling path 210 (comprising the sampling drive 250, the sampling volume 255, and the sampling unit 260), as provided and operated by the switching unit 200, in an overview schematic representation.
  • Figure 3A corresponds to Figure 2A illustrating the load (and preferably pressurisation) configuration allowing to load the fluidic sample into the sampling volume 255 and preferably precompressing the fluidic sample, for example to a pressure range of the mobile phase.
  • the mobile phase drive 20 is fluidically coupled with and driving the mobile phase through the separating device 30.
  • the sampling path 210 and the high-pressure path of the mobile phase between the mobile phase drive 20 and the separating device 30 are fluidically decoupled and separated from each other.
  • Figure 3B corresponds to Figure 2B illustrating the couple configuration, wherein one end of the sampling path 210 is coupling at a coupling point 300 (corresponding to the coupling point provided by ports 2-4 in Figures 2) within the high-pressure path of the mobile phase between the mobile phase drive 20 and the separating device 30.
  • the separating device 30 remains fluidically coupled with the mobile phase drive 20.
  • a pressure equilibration of the pressure within the sampling path 210 with a pressure of the mobile phase (at the coupling point 300) can be provided, for example in order to pressurise (i.e. to increase pressure of) the fluidic sample contained in the sampling volume 255.
  • the couple configuration can be applied for providing Feed-Injection sample introduction of fluidic sample into the mobile phase by combining a flow from the sampling path 210 (preferably driven by the sampling drive 250) with a flow of the mobile phase driven by the mobile phase drive 20 and providing the combined flow towards the separating device 30.
  • Figure 3C corresponds to Figure 2C illustrating the decouple configuration wherein the sampling path 210 is fluidically coupled to the separating device 30, while the mobile phase drive 20 is fluidically decoupled.
  • the configuration of Figure 3C corresponds to the configuration of Figure 3B, however, with the difference that in Figure 3C the mobile phase drive 20 is fluidically decoupled or separated.
  • the separating device 30 remains coupled with the sampling path 210 and thus with the sampling drive 250.
  • Figure 3D corresponds to Figure 2D illustrating the sample introduction configuration for providing flow-through injection.
  • the sampling path 210 (either with or without the sampling drive 250) is coupled between the mobile phase drive 20 and the separating device 30, so that a flow of mobile phase is driven by the mobile phase drive 20 first through the sampling path 210 and then through the separating device 30, so that the mobile phase transports the fluidic sample contained in the sampling volume 255 through the separating device 30 for chromatographic separation.
  • the separating device 30 remains coupled with the sampling path 210 and thus with the sampling drive 250.
  • the separating device 30 in all of the configurations of Figures 2 and 3 is always fluidically coupled with at least one “upstream unit”, i.e. with either the mobile phase drive 20, the sampling path 210, with both.
  • the flow to the separating device 30 is always maintained and may be controlled to provide a flow towards the separating device 30 (for example “actively” by operation of the mobile phase drive 20, by operation of the sampling drive 250, and/or “passively” by applying a pressure to the sampling path 210 exceeding a pressure of the mobile phase between the switching unit 200 and the separating device 30).
  • the switching unit 200 of the exemplary embodiments of Figures 2 and 3 provide a “make before break” switching by providing a continuous fluidic coupling of and to the separating device 30 in all switching states.
  • Figures 4 illustrate another exemplary embodiment of the switching unit 200.
  • Figure 4A shows, represented in accordance with Figure 2E, the stator 220 and the rotor 225 separated from each other for the sake of better understanding.
  • the differences of the embodiment shown in Figure 4A over the embodiment shown in Figure 2E are the following: is the embodiment of Figure 4A, the stator 220 comprises a further stator groove 400 and a fifth port 5, port 2 is at a slightly different location, and the second rotor groove 245 of the rotor 225 is shorter. More precisely, the further stator groove 400 extends from port 2 towards port 3 from about 155° to 185°, port 2 is located at 185°, and the second groove 245 extends also about 75° (as the first groove 240).
  • the further stator groove 400 allows reducing overhanging rotor groove (e.g. the second groove 245) in the Feed-Injection configuration, which may help reducing cavities in order to reduce carry over and sample dispersion.
  • Figure 4B exemplarily illustrates the decouple configuration corresponding to Figure 2C and Figure 3C.
  • Other switching configurations such as shown and described in detail with respect to Figures 2A-2D can be assumed by rotation of the rotor 225 and need not be further detailed here.
  • the coupling of the various components is substantially identical as shown in Figure 2C, however, with the difference that a flush pump 410 is coupled to port 5.
  • the separating device 30 remains fluidically coupled with at least one of the mobile phase drive 20 and the sampling drive 250 during switching from the sample load configuration to the couple configuration, during switching from the couple configuration to the decouple configuration, as well as during switching from the decouple configuration to the sample introduction configuration.
  • the rotor 225 can be rotated (in clockwise direction with respect to Figure 2B) so that the second groove 245 couples between ports 5 and 2.
  • the first groove 240 couples between ports 3 and 4 thus fluidically coupling the mobile phase drive 20 with the separating device 30.
  • the sampling path 210 may comprise a retaining unit, such as a trapping column, having a certain retaining property.
  • Reversing the flow direction through the sampling volume/or the retaining unit may allow, for example, increasing the lifetime of the retaining unit, e.g. by avoiding or reducing plugging, and/or increasing the performance of the retaining unit.

Landscapes

  • Physics & Mathematics (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Sampling And Sample Adjustment (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

L'invention divulgue une unité de commutation (200) conçue pour raccorder fluidiquement de manière sélective un volume d'échantillonnage (255), un entraînement d'échantillonnage (250), un entraînement de phase mobile (20) et un dispositif de séparation (30). L'entraînement de phase mobile (20) est conçu pour entraîner une phase mobile, le dispositif de séparation (30) est conçu pour séparer un échantillon fluidique lorsqu'il est compris dans la phase mobile, le volume d'échantillonnage (255) est conçu pour stocker temporairement l'échantillon fluidique, et l'entraînement d'échantillonnage (250) est conçu pour déplacer un fluide. Dans une configuration de chargement d'échantillon (Figures 2A, 3A), l'unité de commutation (200) est conçue pour raccorder fluidiquement le volume d'échantillonnage (255) et l'entraînement d'échantillonnage (250), à des fins de déplacement de l'échantillon fluidique dans le volume d'échantillonnage (255). Dans une configuration de déraccordement (Figures 2C, 3C), l'unité de commutation (200) est conçue pour raccorder fluidiquement le volume d'échantillonnage (255) entre l'entraînement d'échantillonnage (250) et le dispositif de séparation (30), tandis que l'entraînement de phase mobile (20) est déraccordé fluidiquement du dispositif de séparation (30). Dans une configuration d'introduction d'échantillon (Figures 2D, 3D), l'unité de commutation (200) est conçue pour raccorder fluidiquement l'entraînement de phase mobile (20), le volume d'échantillonnage (255) et le dispositif de séparation (30) pour introduire au moins une quantité de l'échantillon fluidique stocké dans le volume d'échantillonnage (255) dans la phase mobile à des fins de séparation de fluide par le dispositif de séparation (30). Le dispositif de séparation (30) est raccordé fluidiquement à l'entraînement de phase mobile (20) et/ou l'entraînement d'échantillonnage (250) pendant la commutation de la configuration de chargement d'échantillon à la configuration de déraccordement, et pendant la commutation de la configuration de déraccordement à la configuration d'introduction d'échantillon.
PCT/IB2022/054575 2021-05-21 2022-05-17 Raccordement fluidique de trajets d'échantillonnage et de séparation WO2022243867A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB2107310.1A GB2607021A (en) 2021-05-21 2021-05-21 Fluidically coupling of sampling and separation paths
GB2107310.1 2021-05-21

Publications (2)

Publication Number Publication Date
WO2022243867A2 true WO2022243867A2 (fr) 2022-11-24
WO2022243867A3 WO2022243867A3 (fr) 2022-12-29

Family

ID=76637777

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2022/054575 WO2022243867A2 (fr) 2021-05-21 2022-05-17 Raccordement fluidique de trajets d'échantillonnage et de séparation

Country Status (2)

Country Link
GB (1) GB2607021A (fr)
WO (1) WO2022243867A2 (fr)

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0309596A1 (fr) 1987-09-26 1989-04-05 Hewlett-Packard GmbH Dispositif de pompage pour délivrer un liquide à haute pression
US4982597A (en) 1988-06-07 1991-01-08 Hewlett-Packard Company Restrictor heating in supercritical fluid chromatography
EP1577012A1 (fr) 2004-03-08 2005-09-21 Agilent Technologies, Inc. Réceptacle pour puce microfluidique
US8047060B2 (en) 2005-01-31 2011-11-01 Waters Technologies Corporation Method and apparatus for sample injection in liquid chromatography
WO2014199198A1 (fr) 2013-06-12 2014-12-18 Agilent Technologies, Inc. Rincage de dispositif de mesure apte a commuter entre differents trajets fluidiques par un solvant provenant d'un trajet d'analyse d'un systeme de separation de fluides
US20160334031A1 (en) 2014-12-12 2016-11-17 Agilent Technologies, Inc. Uninterrupted fluid flow while modulating fluid
US20170343520A1 (en) 2016-05-30 2017-11-30 Agilent Technologies, Inc. Branching off fluidic sample with low influence on source flow path

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102460145B (zh) * 2009-06-03 2015-04-29 安捷伦科技有限公司 使中间阀状态的压力差平衡的计量装置的样品注射器
DE202016100451U1 (de) * 2015-06-25 2016-02-16 Dionex Softron Gmbh Probengeber für die Flüssigkeitschromatographie, insbesondere für die Hochleistungsflüssigkeitschromatographie
DE102016101658B4 (de) * 2016-01-29 2018-04-05 Dionex Softron Gmbh Probenvorkompressionsventil für die Flüssigkeitschromatographie, insbesondere für die Hochleistungsflüssigkeitschromatographie
EP3252464B1 (fr) * 2016-05-30 2024-03-27 Agilent Technologies, Inc. (A Delaware Corporation) Injecteur et méthode pour l'injection d'échantillon ayant une connexion fluidique entre une unité d'entraînement de fluide et un volume de réception d'échantillon
US11255465B2 (en) * 2016-11-30 2022-02-22 Agilent Technologies, Inc. Microfluidic check valve and related devices and systems
US11635412B2 (en) * 2018-04-06 2023-04-25 Agilent Technologies, Inc Pressure decoupling fluid drive unit from flow path for pressure adjustment of sample accommodation volume
GB2586064B (en) * 2019-08-01 2022-01-12 Agilent Technologies Inc Sample dispatching with fluidic sample retaining

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0309596A1 (fr) 1987-09-26 1989-04-05 Hewlett-Packard GmbH Dispositif de pompage pour délivrer un liquide à haute pression
US4982597A (en) 1988-06-07 1991-01-08 Hewlett-Packard Company Restrictor heating in supercritical fluid chromatography
EP1577012A1 (fr) 2004-03-08 2005-09-21 Agilent Technologies, Inc. Réceptacle pour puce microfluidique
US8047060B2 (en) 2005-01-31 2011-11-01 Waters Technologies Corporation Method and apparatus for sample injection in liquid chromatography
WO2014199198A1 (fr) 2013-06-12 2014-12-18 Agilent Technologies, Inc. Rincage de dispositif de mesure apte a commuter entre differents trajets fluidiques par un solvant provenant d'un trajet d'analyse d'un systeme de separation de fluides
US20160334031A1 (en) 2014-12-12 2016-11-17 Agilent Technologies, Inc. Uninterrupted fluid flow while modulating fluid
US20170343520A1 (en) 2016-05-30 2017-11-30 Agilent Technologies, Inc. Branching off fluidic sample with low influence on source flow path

Also Published As

Publication number Publication date
WO2022243867A3 (fr) 2022-12-29
GB202107310D0 (en) 2021-07-07
GB2607021A (en) 2022-11-30

Similar Documents

Publication Publication Date Title
US11519884B2 (en) Sample injector with metering device balancing pressure differences in an intermediate valve state
EP3252464B1 (fr) Injecteur et méthode pour l'injection d'échantillon ayant une connexion fluidique entre une unité d'entraînement de fluide et un volume de réception d'échantillon
US9823226B2 (en) HPLC sample introduction with coupling sample reservoirs in parallel between mobile phase drive and separation unit
EP3008463A1 (fr) Rincage de dispositif de mesure apte a commuter entre differents trajets fluidiques par un solvant provenant d'un trajet d'analyse d'un systeme de separation de fluides
US20210389282A1 (en) Injector Serving Multiple Sample Separation Apparatuses
US11630090B2 (en) Sample dispatching with fluidic sample retaining
US20210055268A1 (en) Sample handling and dispatching individual sample packages
US10953345B2 (en) HPLC sample introduction with bypass channel
GB2588635A (en) Sample injector with fluidic sample mixing
WO2022243867A2 (fr) Raccordement fluidique de trajets d'échantillonnage et de séparation
US20240241086A1 (en) Fluidically coupling of sampling and separation paths
GB2591435A (en) Sample injection in a combined chromatography system
US20230039500A1 (en) Fluid separation with sampling unit selectively coupling upstream and downstream of separation unit
CN111902718B (zh) 样品分离设备和操作样品分离设备的方法
GB2597469A (en) Pressurizing fluid by expanding membrane
WO2024033691A1 (fr) Mélangeur dans un chemin d'injecteur pour mélange de la phase mobile
CN113227783A (zh) 配置注入器来仿效另一注入器的运行

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 22726823

Country of ref document: EP

Kind code of ref document: A2

WWE Wipo information: entry into national phase

Ref document number: 18562216

Country of ref document: US

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 22726823

Country of ref document: EP

Kind code of ref document: A2